Kindlin-2 is required for myocyte elongation and is essential for myogenesis

BMC Cell Biol. 2008 Jul 8;9:36. doi: 10.1186/1471-2121-9-36.

Abstract

Background: Integrins are required for normal muscle differentiation and disruptions in integrin signaling result in human muscle disease. The intracellular components that regulate integrin function during myogenesis are poorly understood. Unc-112 is an integrin-associated protein required for muscle development in C. elegans. To better understand the intracellular effectors of integrin signaling in muscle, we examined the mammalian homolog of Unc-112, kindlin-2.

Results: Kindlin-2 expression is upregulated during differentiation and highly enriched at sites of integrin localization. RNAi knockdown of kindlin-2 in C2C12 cells results in significant abnormalities during the early stages of myogenesis. Specifically, differentiating myocytes lacking kindlin-2 are unable to elongate and fail to fuse into multinucleated myotubes. These changes are correlated with decreased cell substratum adhesion and increased cell motility. They are also associated with redistribution of a known kindlin-2 binding partner, integrin linked kinase (ILK), to the membrane insoluble subcellular fraction.

Conclusion: In all, our study reveals kindlin-2 as a novel integrin adaptor protein important for muscle differentiation, and identifies it particularly as a critical regulator of myocyte elongation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans Proteins
  • Cell Adhesion
  • Cell Adhesion Molecules
  • Cell Differentiation
  • Cell Line
  • Cell Shape
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / physiology*
  • Integrins
  • Mice
  • Muscle Cells / cytology*
  • Muscle Development*
  • Muscle Fibers, Skeletal
  • Muscle Proteins / genetics
  • Muscle Proteins / physiology*
  • Protein-Serine-Threonine Kinases / metabolism
  • Up-Regulation

Substances

  • Caenorhabditis elegans Proteins
  • Cell Adhesion Molecules
  • Cytoskeletal Proteins
  • Integrins
  • Muscle Proteins
  • UNC-112 protein, C elegans
  • kindlin-2 protein, mouse
  • integrin-linked kinase
  • Protein-Serine-Threonine Kinases